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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1919 2
1950 1
2007 3
2008 1
2011 5
2012 3
2013 5
2014 4
2015 4
2016 6
2017 9
2018 6
2019 4
2020 4
2021 3
2022 1
2023 1
2024 0

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52 results

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Page 1
A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct from Kabuki syndrome.
Cuvertino S, Hartill V, Colyer A, Garner T, Nair N, Al-Gazali L, Canham N, Faundes V, Flinter F, Hertecant J, Holder-Espinasse M, Jackson B, Lynch SA, Nadat F, Narasimhan VM, Peckham M, Sellers R, Seri M, Montanari F, Southgate L, Squeo GM, Trembath R, van Heel D, Venuto S, Weisberg D, Stals K, Ellard S; Genomics England Research Consortium; Barton A, Kimber SJ, Sheridan E, Merla G, Stevens A, Johnson CA, Banka S. Cuvertino S, et al. Among authors: colyer a. Genet Med. 2020 May;22(5):867-877. doi: 10.1038/s41436-019-0743-3. Epub 2020 Jan 17. Genet Med. 2020. PMID: 31949313 Free PMC article.
Structural basis of rotavirus RNA chaperone displacement and RNA annealing.
Bravo JPK, Bartnik K, Venditti L, Acker J, Gail EH, Colyer A, Davidovich C, Lamb DC, Tuma R, Calabrese AN, Borodavka A. Bravo JPK, et al. Among authors: colyer a. Proc Natl Acad Sci U S A. 2021 Oct 12;118(41):e2100198118. doi: 10.1073/pnas.2100198118. Proc Natl Acad Sci U S A. 2021. PMID: 34615715 Free PMC article.
Structure of dual BON-domain protein DolP identifies phospholipid binding as a new mechanism for protein localisation.
Bryant JA, Morris FC, Knowles TJ, Maderbocus R, Heinz E, Boelter G, Alodaini D, Colyer A, Wotherspoon PJ, Staunton KA, Jeeves M, Browning DF, Sevastsyanovich YR, Wells TJ, Rossiter AE, Bavro VN, Sridhar P, Ward DG, Chong ZS, Goodall EC, Icke C, Teo AC, Chng SS, Roper DI, Lithgow T, Cunningham AF, Banzhaf M, Overduin M, Henderson IR. Bryant JA, et al. Among authors: colyer a. Elife. 2020 Dec 14;9:e62614. doi: 10.7554/eLife.62614. Elife. 2020. PMID: 33315009 Free PMC article.
52 results